5OWL
Low salt structure of human protein kinase CK2alpha in complex with 3-aminopropyl-4,5,6,7-tetrabromobenzimidazol
Summary for 5OWL
Entry DOI | 10.2210/pdb5owl/pdb |
Related | 5OWH |
Descriptor | Casein kinase II subunit alpha, 3-[4,5,6,7-tetrakis(bromanyl)benzimidazol-1-yl]propan-1-amine, SULFATE ION, ... (5 entities in total) |
Functional Keywords | protein kinase ck2 casein kinase 2 atp-competitive inhibitor 3-aminopropyl-4, 5, 6, 7-tetrabromobenzimidazol, transferase |
Biological source | Homo sapiens (Human) |
Total number of polymer chains | 2 |
Total formula weight | 81687.52 |
Authors | Niefind, K.,Bretner, M.,Chojnacki, C. (deposition date: 2017-09-01, release date: 2018-07-25, Last modification date: 2024-01-17) |
Primary citation | Chojnacki, K.,Winska, P.,Wielechowska, M.,Lukowska-Chojnacka, E.,Tolzer, C.,Niefind, K.,Bretner, M. Biological properties and structural study of new aminoalkyl derivatives of benzimidazole and benzotriazole, dual inhibitors of CK2 and PIM1 kinases. Bioorg. Chem., 80:266-275, 2018 Cited by PubMed: 29966873DOI: 10.1016/j.bioorg.2018.06.022 PDB entries with the same primary citation |
Experimental method | X-RAY DIFFRACTION (2.23 Å) |
Structure validation
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